Canonical Allele Identifier: CA2840565076

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74501040dup , CM000676.2:g.74501040dup	GRCh38
NC_000014.8:g.74967743dup , CM000676.1:g.74967743dup	GRCh37
NC_000014.7:g.74037496dup	NCBI36
NG_021486.1:g.116294dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5321-9dup MANE Select	ENSP00000261978.4:n.5321-9dup
ENST00000261978.8:c.5321-9dup	ENSP00000261978.4:n.5321-9dup
ENST00000553939.5:c.*100-9dup	ENSP00000452110.1:n.*100-9dup
ENST00000554861.1:n.539-9dup
ENST00000556690.5:c.5189-9dup	ENSP00000451477.1:n.5189-9dup
NM_000428.2:c.5321-9dup	NP_000419.1:n.5321-9dup
XM_011536765.1:c.4940-9dup	XP_011535067.1:n.4940-9dup
XM_011536766.1:c.4862-9dup	XP_011535068.1:n.4862-9dup
XM_011536767.1:c.4838-9dup	XP_011535069.1:n.4838-9dup
XM_011536765.2:c.4940-9dup	XP_011535067.1:n.4940-9dup
NM_000428.3:c.5321-9dup MANE Select	NP_000419.1:n.5321-9dup